US20120214885A1 - Foamable polystyrene resin particles and process for production thereof, polystyrene resin prefoamed particles, polystyrene resin foam-molded article, heat-insulating material for building material, banking member, and vehicle interior material - Google Patents

Foamable polystyrene resin particles and process for production thereof, polystyrene resin prefoamed particles, polystyrene resin foam-molded article, heat-insulating material for building material, banking member, and vehicle interior material Download PDF

Info

Publication number
US20120214885A1
US20120214885A1 US13/504,072 US201013504072A US2012214885A1 US 20120214885 A1 US20120214885 A1 US 20120214885A1 US 201013504072 A US201013504072 A US 201013504072A US 2012214885 A1 US2012214885 A1 US 2012214885A1
Authority
US
United States
Prior art keywords
polystyrene resin
flame retardant
resin particles
foamable polystyrene
producing
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US13/504,072
Other languages
English (en)
Inventor
Hiroyuki Tarumoto
Ryosuke Chinomi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sekisui Kasei Co Ltd
Original Assignee
Sekisui Plastics Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP2009246290A external-priority patent/JP5750221B2/ja
Priority claimed from JP2009246293A external-priority patent/JP2011093950A/ja
Priority claimed from JP2009246291A external-priority patent/JP2011093948A/ja
Priority claimed from JP2009246292A external-priority patent/JP2011093949A/ja
Application filed by Sekisui Plastics Co Ltd filed Critical Sekisui Plastics Co Ltd
Assigned to SEKISUI PLASTICS CO., LTD. reassignment SEKISUI PLASTICS CO., LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CHINOMI, RYOSUKE, TARUMOTO, HIROYUKI
Publication of US20120214885A1 publication Critical patent/US20120214885A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0014—Use of organic additives
    • C08J9/0019—Use of organic additives halogenated
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B7/00—Mixing; Kneading
    • B29B7/30—Mixing; Kneading continuous, with mechanical mixing or kneading devices
    • B29B7/58—Component parts, details or accessories; Auxiliary operations
    • B29B7/582—Component parts, details or accessories; Auxiliary operations for discharging, e.g. doors
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B9/00—Making granules
    • B29B9/02—Making granules by dividing preformed material
    • B29B9/06—Making granules by dividing preformed material in the form of filamentary material, e.g. combined with extrusion
    • B29B9/065—Making granules by dividing preformed material in the form of filamentary material, e.g. combined with extrusion under-water, e.g. underwater pelletizers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B9/00—Making granules
    • B29B9/12—Making granules characterised by structure or composition
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/22—After-treatment of expandable particles; Forming foamed products
    • C08J9/228—Forming foamed products
    • C08J9/232—Forming foamed products by sintering expandable particles
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/13—Phenols; Phenolates
    • C08K5/136—Phenols containing halogens
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2203/00—Foams characterized by the expanding agent
    • C08J2203/14—Saturated hydrocarbons, e.g. butane; Unspecified hydrocarbons
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2325/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
    • C08J2325/02—Homopolymers or copolymers of hydrocarbons
    • C08J2325/04—Homopolymers or copolymers of styrene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00—Specific properties of additives
    • C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
    • C08K3/016—Flame-proofing or flame-retarding additives
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00—Properties
    • C08L2201/02—Flame or fire retardant/resistant
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00—Applications
    • C08L2203/14—Applications used for foams

Definitions

  • the present invention relates to a polystyrene resin foam-molded article excellent in environmental compatibility and flame retardancy, and to foamable polystyrene resin particles used for producing the molded product and a process for production thereof.
  • the polystyrene resin foam-molded article of the present invention is suitably used for a foam-molded article which is required to have flame retardancy, for example, for building materials, members for banking, vehicle interior materials, and the like.
  • Priorities are claimed on Japanese Patent Application Nos. 2009-246290, 2009-246291, 2009-246292, and 2009-246293 filed Oct. 27, 2009, the content of which is incorporated herein by reference.
  • the polystyrene resin particles according to the present invention are specifically flame retardant-containing polystyrene resin particles, foamable polystyrene resin particles for producing a heat-insulating material for building materials, foamable polystyrene resin particles for producing a banking member, and foamable polystyrene resin particles for producing a vehicle interior material.
  • foamable polystyrene resin particles for producing a heat-insulating material for building materials
  • foamable polystyrene resin particles for producing a banking member foamable polystyrene resin particles for producing a vehicle interior material.
  • Patent Document 1 discloses a process for producing a flame-retarding foamed styrene-based resin, which includes adding an organic solvent solution that contains 1.0 part by mass to 10 parts by mass of a bromine-based flame retardant having a predetermined structure and a foaming agent to 100 parts by mass of a styrene-based resin, and heating and foaming this mixture.
  • Patent Document 2 discloses a process for producing a self-extinguishing polystyrene resin particles, which is characterized by including dispersing tetrabromobisphenol A diallyl ether such that the particle size becomes 50 ⁇ m or less in the presence of a surfactant, and then impregnating polystyrene resin particles with this dispersion as well as a softening agent, a flame-retarding aid, a plasticizer, and a foaming agent.
  • Patent Document 2 also discloses a molded article obtained using the resin particles.
  • Patent Document 3 discloses a particle-like expandable styrene polymer containing evenly distributed graphite powder, and self-extinguishing foam obtained by treating the polymer. Patent Document 3 also discloses that the treatment can produce self-extinguishing foam which contains, as a flame retardant, an organic bromine compound including 70% by mass or more of bromine and passes a combustion test B2 (according to DIN 4102).
  • an organic bromine compound including 70% by mass or more of bromine and passes a combustion test B2 (according to DIN 4102).
  • the organic bromine compound hexabromocyclododecane, pentabromomonochlorocyclohexane, and pentabromophenylallyl ether are disclosed.
  • an insulation method in order to improve an insulation performance in houses and the like, heat-insulating materials are installed between joists in a floor or between supporting members such as pillars or stud walls.
  • heat-insulating materials used for such an insulation method, glass wool has been widely used in general.
  • the insulating effect of glass wool easily deteriorates since glass wool is hygroscopic. Accordingly, a high insulating effect over a long time cannot be expected, and there are problems in workability.
  • this type of insulating material has begun to be substituted with a polystyrene resin foam-molded article that is excellent in dimensional stability and a heat-insulating property.
  • the heat-insulating material for building materials is generally required to have a flame-retarding performance of a certain level or higher, from the viewpoints of preventing fire or the like, preventing spread of fire resulting from flame spreading in fire, and the like.
  • a flame retardant is used by being added to foamable polystyrene resin particles for producing foamed molded articles.
  • the insulating material for building materials is required to have a water proofing property, an anti-hygroscopic property, moisture resistance, and a heat-insulating property. Moreover, the insulating material is also required not to expand or contract with temperature change (dimensional stability).
  • the insulating material for building materials is required to reduce the amount of volatile organic compounds released.
  • causative compounds of sick house syndrome include, as volatile organic compounds (VOC) for which the Ministry of Health, Labour and Welfare has established a guideline amount, formaldehyde, acetaldehyde, toluene, xylene, ethylbenzene, styrene, and the like.
  • Patent Document 4 As foamable polystyrene resin particles used as insulating materials for building materials, for example, a technique disclosed in Patent Document 4 has been suggested in the related art.
  • Patent Document 4 discloses foamable polystyrene resin particles which contain, in 100 parts by mass of foamable polystyrene resin particles, 350 ppm to 1200 ppm of a styrene monomer, 0.1 parts by mass to 2 parts by mass of a plasticizer that cannot be distilled at 250° C. or lower when vacuum distillation is performed under a pressure of 6.666 ⁇ 10 ⁇ 4 MPa (5 mmHg), and a foaming agent.
  • foamed synthetic resin blocks has been widely used as the bank on weak ground, for slopes, or for an artificial hill in a garden, and used for embedding or backfilling of an underground structure.
  • foam used for these members polystyrene resin foams are used in many cases from the viewpoints of strength, water resistance, and the like.
  • foamed molded articles are generally used which are produced in an in-mold foam molding method which includes pre-foaming foamable polystyrene resin particles (also referred to as beads) by heating, filling the obtained prefoamed particles in a cavity of a mold, and performing foaming by heating and molding in the mold.
  • the banking member is generally required to have a flame-retarding performance of a certain level or higher, from the viewpoints of preventing fire or the like, preventing the ground from becoming unstable due to flame spreading, and the like.
  • a flame retardant is used by being added to the foamable polystyrene resin particles for producing the foamed molded article.
  • interior materials of various vehicles such as automobiles
  • synthetic resin products have been widely used.
  • vehicle interior materials formed of synthetic resin foam-molded article are widely used, for the purposes of improving ride comfort by enhancing shock absorbing properties, protecting passengers by absorbing shock, securing flatness in a vehicle, and the like.
  • foam-molded articles various resins such as foamable urethane and foamable polystyrene are used.
  • foamable polystyrene resin is widely used since this resin is excellent in moldability and functionality.
  • examples of vehicle interior materials using the foamable polystyrene resin include automobile interior materials, particularly, a floor spacer, a door pad, a toolbox, and the like.
  • the vehicle interior material is generally required to have a flame-retarding performance of a certain level or higher, from the viewpoints of preventing fire or the like and a self-extinguishing property.
  • a flame retardant is used by being added to foamable polystyrene resin particles for producing the foam-molded article.
  • the vehicle interior materials are strongly required to contain an extremely small amount of volatile organic compounds.
  • Patent Document 8 a technique disclosed in Patent Document 8 has been suggested.
  • Patent Document 8 discloses styrene-based foamable resin particles which contain 1 ppm to 300 ppm of a residual styrene monomer, 1 ppm or less of benzene, 0.1% by mass to 2% by mass of a plasticizer that is compatible with styrene and has an SP value of 7 to 10, and a foaming agent.
  • Patent Document 4 discloses foamable polystyrene resin particles which contain, in 100 parts by mass of the foamable polystyrene resin particles, 350 ppm to 1200 ppm of a styrene monomer, 0.1 parts by mass to 2 parts by mass of a plasticizer that cannot be distilled at 250° C. or lower when vacuum distillation is performed under a pressure of 6.666 ⁇ 10 ⁇ 4 MPa (5 mmHg), and a foaming agent.
  • Patent Document 4 Japanese Patent Application, First Publication No. 2003-64212
  • the flame retardant is supplied to an extruder or an autoclave by being dissolved in advance in an organic solvent.
  • a volatile solvent in a step of dissolving the flame retardant in an organic solvent is not preferable since this exerts a serious negative influence on the environment, and the foam-molded article generates volatile organic compounds (VOC).
  • VOC volatile organic compounds
  • the foaming agent is volatilized, so the working environment deteriorates.
  • the flame retardant is dispersed such that the particle size thereof becomes 50 ⁇ m or less in the presence of a surfactant, and then polystyrene resin particles are impregnated with this dispersion as well as a softening agent, a flame-retarding aid, a plasticizer, and a foaming agent, thereby producing flame retardant-containing foamable polystyrene resin particles.
  • the flame retardant is absent in the vicinity of the center of the resin particles, or only flame retardant-containing foamable polystyrene resin particles which contain a small amount of the flame retardant are obtained. Consequently, the mechanical strength of a flame-retarding polystyrene resin foam-molded article that is obtained by pre-foaming such resin particles and performing in-mold foam molding on the obtained prefoamed particles deteriorates, and the moldability and exterior thereof deteriorate.
  • an organic bromine compound such as hexabromocyclododecane is used as a flame retardant.
  • hexabromocyclododecane is a type 1 monitored chemical substance in the Chemical Substances Control Law. The persistency and high enrichment of this compound were pointed out by the safety inspection for existing chemical substances conducted by the Ministry of Economy, Trade and Industry, and this compound corresponds to an evaluation object of risk assessment in Europe. In this way, this compound has problems in safety, so there is a demand for not using this compound. Therefore, in the future, it will be difficult to use this type of organic bromine compound in the field of flame-retarding polystyrene resin foam-molded article.
  • Patent Document 4 discloses a suspension polymerization method as a specific process for producing the foamable polystyrene resin particles.
  • hexabromocyclododecane participates in the whole styrene polymerization process.
  • hexabromocyclododecane hinders polymerization of styrene monomers. Consequently, the obtained foamable polystyrene resin particles contain a large amount of residual volatile organic compounds, which makes it difficult to counteract the sick house syndrome as desired recently. Therefore, hexabromocyclododecane is not suitable for producing heat-insulating materials for building materials or vehicle interior materials.
  • the powdered flame retardant undergoes secondary agglomeration in a suspension, whereby the flame retardant is unevenly dispersed in the suspension. Consequently, the powdered flame retardant is unevenly absorbed in the resin particles, so a portion of the resin particles absorbs a large amount of the flame retardant.
  • the flame retardant is absent in the vicinity of the center of the resin particles, or only resin particles which contain a small amount of the flame retardant is obtained.
  • the mechanical strength of a polystyrene resin foam-molded article that is obtained by pre-foaming such resin particles and performing in-mold foam molding on the obtained prefoamed particles deteriorates, the dimensional stability is reduced, and the moldability and the exterior deteriorate. Accordingly, this molded article is not suitable for producing members for banking or vehicle interior materials.
  • the present invention has been made in consideration of the above circumstances, and an object thereof is to provide a flame-retarding polystyrene resin foam-molded article which uses a flame retardant that is highly safe for the environment and living organisms, has a sufficient flame-retarding performance, and is excellent in the mechanical strength, moldability, exterior, and dimensional stability, a heat-insulating material for building materials, a banking member, and a vehicle interior material.
  • the present invention provides flame retardant-containing foamable polystyrene resin particles that are obtained by granulating a polystyrene resin containing a flame retardant and a foaming agent, wherein the flame retardant has a bromine atom in a molecule, contains less than 70% by mass of bromine, has a benzene ring in a molecule, and has a 5% by mass decomposition temperature in a range of from 200° C.
  • the flame retardant-containing foamable polystyrene resin particles of the present invention are preferably obtained in a melt extrusion method in which the flame retardant-containing foamable polystyrene resin particles are obtained by adding a flame retardant and a foaming agent to a polystyrene resin and kneading this mixture in a resin supply device, extruding the molten resin containing the flame retardant and the foaming agent directly into a cooling liquid from small holes of a die that is attached to the leading end of the resin supply device, cutting the extrudate simultaneously with the extrusion, and cooling and solidifying the extrudate by bringing the extrudate into contact with the liquid.
  • the present invention provides flame-retarding polystyrene resinprefoamed particles that are obtained by heating the flame retardant-containing foamable polystyrene resin particles.
  • the present invention also provides a flame-retarding polystyrene resin foam-molded article that is obtained by filling a cavity of a mold with the flame-retarding polystyrene resinprefoamed particles and heating and foaming the particles.
  • the present invention provides foamable polystyrene resin particles for producing a heat-insulating material for building materials that are obtained by granulating a polystyrene resin containing a flame retardant and a foaming agent, wherein the flame retardant has a bromine atom in a molecule, contains less than 70% by mass of bromine, has a benzene ring in a molecule, and has a 5% by mass decomposition temperature in a range of from 200° C.
  • the foamable polystyrene resin particles for producing a heat-insulating material for building materials are obtained by a melt extrusion method in which the foamable polystyrene resin particles for producing a heat-insulating material for building materials are obtained by adding the flame retardant and the foaming agent to the polystyrene resin and kneading this mixture in a resin supply device, extruding the molten resin containing the flame retardant and the foaming agent directly into a cooling liquid from small holes of a die that is attached to the leading end of the resin supply device, cutting the extrudate simultaneously with the extrusion, and cooling and solidifying the extrudate by bringing the extrudate into contact with the liquid.
  • the total amount of contained aromatic organic compounds including a styrene-based monomer, ethylbenzene, isopropylbenzene, normalpropylbenzene, xylene, toluene, and benzene is preferably less than 500 ppm.
  • the present invention also provides prefoamed particles for producing a heat-insulating material for building materials that are obtained by heating the foamable polystyrene resin particles for producing a heat-insulating material for building materials.
  • the present invention provides a heat-insulating material for building materials that is obtained by filling a cavity of a mold with the prefoamed particles for producing a heat-insulating material for building materials and heating and foaming the particles, wherein the density is in a range of from 0.010 g/cm 3 to 0.050 g/cm 3 .
  • the present invention also provides a heat-insulating material for building materials that is obtained by filling a cavity of a mold with the prefoamed particles for producing a heat-insulating material for building materials and heating and foaming the particles, wherein in a foam-molded article thereof that is foamed 40-fold in terms of a foaming factor, an average chord length of bubbles is in a range of from 50 ⁇ m to 350 ⁇ m.
  • the present invention provides foamable polystyrene resin particles for producing a banking member that are obtained by granulating a polystyrene resin containing a flame retardant and a foaming agent, wherein the flame retardant has a bromine atom in a molecule, contains less than 70% by mass of bromine, has a benzene ring in a molecule, and has a 5% by mass decomposition temperature in a range of from 200° C.
  • the foamable polystyrene resin particles for producing a banking member are obtained by a melt extrusion method in which the foamable polystyrene resin particles are obtained by adding the flame retardant and the foaming agent to the polystyrene resin and kneading this mixture in a resin supply device, extruding the molten resin containing the flame retardant and the foaming agent directly into a cooling liquid from small holes of a die that is attached to the leading end of the resin supply device, cutting the extrudate simultaneously with the extrusion, and cooling and solidifying the extrudate by bringing the extrudate into contact with the liquid.
  • the present invention also provides prefoamed particles for producing a banking member that are obtained by heating the foamable polystyrene resin particles for producing a banking member.
  • the present invention provides a banking member that is obtained by filling a cavity of a mold with the prefoamed particles for producing a banking member and heating and foaming the particles, wherein the density is in a range of from 0.010 g/cm 3 to 0.050 g/cm 3 .
  • the present invention also provides a banking member that is obtained by filling a cavity of a mold with the prefoamed particles for producing a banking member and heating and foaming the particles, wherein in a foam-molded article thereof that is foamed 50-fold in terms of a foaming factor, an average chord length of bubbles is in a range of from 40 ⁇ m to 200 ⁇ m.
  • the present invention provides a banking member that is obtained by filling a cavity of a mold with the prefoamed particles for producing a banking member and heating and foaming the particles, wherein an oxygen index is 26 or greater.
  • the present invention provides foamable polystyrene resin particles for producing a vehicle interior material that are obtained by granulating a polystyrene resin containing a flame retardant and a foaming agent, wherein the flame retardant has a bromine atom in a molecule, contains less than 70% by mass of bromine, has a benzene ring in a molecule, and has a 5% by mass decomposition temperature in a range of from 200° C.
  • the foamable polystyrene resin particles for producing a vehicle interior material are obtained by a melt extrusion method in which the foamable polystyrene resin particles for producing a vehicle interior material are obtained by adding the flame retardant and the foaming agent to the polystyrene resin and kneading this mixture in a resin supply device, extruding the molten resin containing the flame retardant and the foaming agent directly into a cooling liquid from small holes of a die that is attached to the leading end of the resin supply device, cutting the extrudate simultaneously with the extrusion, and cooling and solidifying the extrudate by bringing the extrudate into contact with the liquid.
  • the total amount of contained aromatic organic compounds including a styrene-based monomer, ethylbenzene, isopropylbenzene, normalpropylbenzene, xylene, toluene, and benzene is preferably less than 500 ppm.
  • the present invention also provides prefoamed particles for producing a vehicle interior material that are obtained by heating the foamable polystyrene resin particles for producing a vehicle interior material.
  • the present invention provides a vehicle interior material that is obtained by filling a cavity of a mold with the prefoamed particles for producing a vehicle interior material and heating and foaming the particles, wherein in a foam-molded article thereof that is foamed 40-fold in terms of a foaming factor, an average chord length of bubbles is in a range of from 40 ⁇ m to 350 ⁇ m.
  • the present invention provides a vehicle interior material that is obtained by obtained by filling a cavity of a mold with the prefoamed particles for producing a vehicle interior material and heating and foaming the particles, wherein the density is in a range of from 0.015 g/cm 3 to 0.066 g/cm 3 .
  • the flame retardant is preferably one or two or more kinds selected from a group consisting of tetrabromobisphenol A and a derivative thereof.
  • the flame retardant is preferably one or two or more kinds selected from a group consisting of tetrabromobisphenol A-bis(2,3-dibromo-2-methylpropyl ether), tetrabromobisphenol A-bis(2,3-dibromopropyl ether), and tetrabromobisphenol A-bis(allyl ether).
  • the present invention also provides a process for producing flame retardant-containing foamable polystyrene resin particles, including adding a flame retardant that has a bromine atom in a molecule, contains less than 70% by mass of bromine, has a benzene ring in a molecule, and has a 5% by mass decomposition temperature in a range of from 200° C. to 300° C.
  • the present invention provides a process for producting foamable polystyrene resin particles for producing a heat-insulating material for building materials, including adding a flame retardant that has a bromine atom in a molecule, contains less than 70% by mass of bromine, has a benzene ring in a molecule, and has a 5% by mass decomposition temperature in a range of from 200° C. to 300° C.
  • foamable polystyrene resin particles are obtained without using aromatic organic compounds including a styrene-based monomer, ethylbenzene, isopropylbenzene, normalpropylbenzene, xylene, toluene, and benzene.
  • the present invention provides a process for producing foamable polystyrene resin particles for producing a banking member, including adding a flame retardant that has a bromine atom in a molecule, contains less than 70% by mass of bromine, has a benzene ring in a molecule, and has a 5% by mass decomposition temperature in a range of from 200° C. to 300° C.
  • the present invention also provides a process for producing foamable polystyrene resin particles for producing a vehicle interior material, including adding a flame retardant that has a bromine atom in a molecule, contains less than 70% by mass of bromine, has a benzene ring in a molecule, and has a 5% by mass decomposition temperature in a range of from 200° C. to 300° C.
  • foamable polystyrene resin particles are obtained without using aromatic organic compounds including a styrene-based monomer, ethylbenzene, isopropylbenzene, normalpropylbenzene, xylene, toluene, and benzene.
  • the flame retardant is preferably one or two or more kinds selected from a group consisting of tetrabromobisphenol A and a derivative thereof.
  • the flame retardant is preferably one or two or more kinds selected from a group consisting of tetrabromobisphenol A-bis(2,3-dibromo-2-methylpropyl ether), tetrabromobisphenol A-bis(2,3-dibromopropyl ether), and tetrabromobisphenol A-bis(allyl ether).
  • a master batch material containing a predetermined level of the flame retardant in a resin be supplied into the resin supply device together with the polystyrene resin, and melted and kneaded in this device.
  • the foamable polystyrene resin particles of the present invention contains a flame retardant that has a bromine atom in a molecule, contains less than 70% by mass of bromine, has a benzene ring in a molecule, and has a 5% by mass decomposition temperature in a range of from 200° C. to 300° C.
  • This flame retardant is highly safe for the environment and living organisms.
  • a tetrabromobisphenol A derivative can impart a sufficient flame-retarding performance, and is highly safe for the environment and living organisms. Accordingly, the flame retardant can be used for producing flame-retarding polystyrene resin foam-molded articles for various uses.
  • a ratio (B/A) between (A) the amount of the flame retardant contained in the total resin particles and (B) the amount of the flame retardant contained in the surface of the resin particles is in a range of from 0.8 to 1.2, so the flame retardant is evenly distributed in the resin particles. Consequently, compared to particles in which the flame retardant is unevenly distributed in the resin particles, the mechanical strength of the obtained polystyrene resin foam-molded article is increased, and the moldability and exterior of the obtained foam-molded article are also superior.
  • the foamable polystyrene resin particles for producing a heat-insulating material for building materials are obtained by a melt extrusion method in which the foamable polystyrene resin particles are obtained by adding a flame retardant and a foaming agent to a polystyrene resin and kneading this mixture in a resin supply device, extruding the molten resin containing the flame retardant and the foaming agent directly into a cooling liquid from small holes of a die that is attached to the leading end of the resin supply device, cutting the extrudate simultaneously with the extrusion, and cooling and solidifying the extrudate by bringing the extrudate into contact with the liquid.
  • the flame retardant is evenly distributed in the resin particles. Therefore, compared to resin particles in which the flame retardant is unevenly distributed in the resin particles, the mechanical strength of the obtained insulating material for building materials, the banking member, and the vehicle interior material increases, and the dimensional stability and moldability of the obtained insulating material for building materials, the banking member, and the vehicle interior material are superior.
  • the polystyrene resin foam-molded article of the present invention is obtained by pre-foaming the foamable polystyrene resin particles by heating, filling the obtained prefoamed particles in a cavity of a mold, and heating and foaming the particles. Accordingly, it is possible to provide flame-retarding polystyrene resin foam-molded articles (a heat-insulating material for building materials, a banking member, and a vehicle interior material) that use a flame retardant which is highly safe for the environment and living organisms, has a sufficient flame-retarding performance, and are excellent in the mechanical strength, moldability, dimensional stability, and exterior.
  • the flame retardant is used by being added in the polystyrene resin, it is possible to reduce the amount of a residual volatile organic compounds such as a styrene-based monomer contained in the foam-molded article. Therefore, the present invention can counteract the sick house syndrome.
  • the process for producing foamable polystyrene resin particles of the present invention it is possible to efficiently produce foamable polystyrene resin particles having excellent effects as described above.
  • the process for producing flame retardant-containing foamable polystyrene resin particles of the present invention it is possible to produce the flame retardant-containing foamable polystyrene resin particles in which (A) the amount of the flame retardant contained in the total resin particles is almost the same as (B) the amount of the flame retardant contained in the surface of the resin particles, and the flame retardant is evenly contained in the resin particles, with a high efficiency.
  • foamable polystyrene resin particles for producing a heat-insulating material for building materials and the process for producing foamable polystyrene resin particles for producing a vehicle interior material of the present invention, it is possible to produce foamable polystyrene resin particles for producing a heat-insulating material for building materials that contain a small amount of aromatic organic compounds including a styrene-based monomer, ethylbenzene, isopropylbenzene, normal propylbenzene, xylene, toluene, and benzene, with a high efficiency.
  • aromatic organic compounds including a styrene-based monomer, ethylbenzene, isopropylbenzene, normal propylbenzene, xylene, toluene, and benzene
  • FIG. 1 is configuration view showing an example of a production apparatus used for the process for producing foamable polystyrene resin particles of the present invention.
  • FIG. 2 is a schematic front view showing a state where the outermost surface portion of the polystyrene resin foam-molded article is cut for example.
  • the foamable polystyrene resin particles are obtained by adding a flame retardant that has a bromine atom in a molecule, contains less than 70% by mass of bromine, has a benzene ring in a molecule, and has a 5% by mass decomposition temperature in a range of from 200° C. to 300° C.
  • FIG. 1 is a configuration view showing an example of a production apparatus used for the process for producing foamable polystyrene resin particles of the present invention.
  • the production apparatus in this example includes an extruder 1 as a resin supply device; a die 2 that is provided at the leading end of the extruder 1 and has many small holes; a raw material supply hopper 3 that introduce a raw material of a resin into the extruder 1 ; a high-pressure pump 4 that pushes a foaming agent into a molten resin in the extruder 1 through a foaming agent supply port 5 ; a cutting chamber 7 which is provided such that cooling water contacts a resin discharge surface of the die 2 where small holes are bored and into which the cooling water is circulatively supplied; a cutter 6 that is rotatably provided in the cutting chamber 7 so as to be able to cut the resin extruded from the small holes of the die 2 ; a dehydrating drier 10 with a solid-liquid separation function that obtains foamable particles by separating foamable
  • any extruder using or not using a screw can be used.
  • extruders using a screw include a single-axis extruder, a multi-axis extruder, a vent-type extruder, a tandem-type extruder, and the like.
  • extruders not using a screw include a plunger-type extruder, a gear pump-type extruder, and the like. All of these extruders can use a static mixer. Among these extruders, extruders using a screw are preferable in terms of productivity.
  • the cutting chamber 7 accommodating the cutter 6 can also use a device known in the related art that has been used in a granulation method implemented by melt extrusion of a resin.
  • the polystyrene resin is not particularly limited.
  • the resin include homopolymers of a styrene-based monomer such as styrene, ⁇ -methylstyrene, vinyltoluene, chlorostyrene, ethylstyrene, i-propylstyrene, dimethylstyrene, or bromostyrene or a copolymer of these, and the like.
  • the polystyrene resin is preferably a polystyrene resin containing 50% by mass or more of styrene, and more preferably polystyrene.
  • the polystyrene resin may be a copolymer that contains the styrene monomer as a main component and is obtained by copolymerzing the styrene-based monomer with a vinyl monomer copolymerizable with the styrene-based monomer.
  • vinyl monomer examples include alkyl (meth)acrylates such as methyl (meth)acrylate, ethyl (meth)acrylate, butyl (meth)acrylate, or cetyl (meth)acrylate, (meth)acrylonitrile, dimethyl maleate, dimethyl fumarate, diethyl fumarate, ethyl fumarate, and bifunctional monomers such as divinylbenzene or alkylene glycol dimethacrylate.
  • alkyl (meth)acrylates such as methyl (meth)acrylate, ethyl (meth)acrylate, butyl (meth)acrylate, or cetyl (meth)acrylate, (meth)acrylonitrile, dimethyl maleate, dimethyl fumarate, diethyl fumarate, ethyl fumarate, and bifunctional monomers such as divinylbenzene or alkylene glycol dimethacrylate.
  • polystyrene resin is a main component
  • other resins may be added.
  • resins to be added include a rubber modified polystyrene resin to which a diene-based rubber-like polymer such as polybutadiene, a styrene-butadiene copolymer, or an ethylene-propylene-unconjugated diene three-dimensional copolymer has been added to improve the impact resistance of foam-molded articles, so-called high impact polystyrene.
  • the examples include a polyethylene-based resin, a polypropylene-based resin, an acrylic resin, an acrylonitrile-styrene copolymer, an acrylonitrile-butadiene-styrene copolymer, and the like.
  • polystyrene resins as the polystyrene resin as a raw material, commercially available general polystyrene resins, polystyrene resins (virgin polystyrene) that are not recyclable raw materials, such as polystyrene resins newly prepared by a method such as a suspension polymerization method can be used. Moreover, recycled raw materials obtained by performing recycling treatment on used polystyrene resin foam-molded articles can also be used.
  • the recycled raw material it is possible to appropriately select a raw material having a weight average molecular weight Mw in a range of from 120,000 to 400,000, from recycled raw materials obtained by recovering used polystyrene resin foam-molded articles, for example, fish boxes, shock-absorbing materials for home appliances, and food packing trays, and recycling the materials by a limonene dissolution method or a heating volume reduction method.
  • a plurality of recycled raw materials differing in the weight average molecular weight Mw by appropriately combining the materials.
  • the flame retardant a flame retardant that has a bromine atom in a molecule, contains less than 70% by mass of bromine, has a benzene ring in a molecule, and has a 5% by mass decomposition temperature in a range of from 200° C. to 300° C. is used.
  • the flame retardant to be used one or two or more kinds of the flame retardants may be mixed, or other flame retardants may be added to the flame retardant as a main component.
  • a flame retardant that contains more than 70% by mass of bromine and does not have a benzene ring in a molecule it is difficult to produce the effect of the present invention that provides flame-retarding polystyrene resin foam-molded articles that are excellent in mechanical strength, moldability, and exterior.
  • the lower limit of the amount of bromine contained is not particularly limited. However, if the amount is 50% by mass or more, a flame-retarding efficiency becomes excellent, which is thus preferable.
  • the more preferable range of the amount of bromine contained is from 55% by mass to 69% by mass.
  • the 5% by mass decomposition temperature of the flame retardant is preferably in a range of from 230° C. to 300° C., more preferably in a range of from 240° C. to 295° C., and most preferably in a range of from 265° C. to 290° C.
  • examples of preferable flame retardants include one or two or more kinds selected from a group consisting of tetrabromobisphenol A and a derivative thereof.
  • these flame retardants one or two or more kinds of flame retardants selected from a group consisting of tetrabromobisphenol A-bis(2,3-dibromo-2-methylpropyl ether), tetrabromobisphenol A-bis(2,3-dibromopropyl ether), and tetrabromobisphenol A-bis(allyl ether) are particularly preferable.
  • tetrabromobisphenol A-bis(2,3-dibromopropyl ether) and tetrabromobisphenol A-bis(2,3-dibromo-2-methylpropyl ether) having a high 5% by mass decomposition temperature are more preferable, and tetrabromobisphenol A-bis(2,3-dibromopropyl ether) is most preferable.
  • the amount of the flame retardant added is preferably in a range of from 0.5% by mass to 8.0% by mass, and more preferably in a range of from 1.0% by mass to 6.0% by mass, based on 100 parts by mass of the resin fraction in the flame retardant-containing foamable polystyrene resin particles. If the amount of the flame retardant added falls short of this range, the flame retardancy of the obtained foam-molded article deteriorates. If the amount of the flame retardant added exceeds this range, there is a possibility that the mechanical strength, moldability, and exterior of the obtained foam-molded article will deteriorate.
  • the foaming agent is not particularly limited.
  • normal pentane, isopentane, cyclopentane, cyclopentadiene, and the like can be used alone, or as a mixture of two or more kinds of these.
  • normal butane, isobutane, propane, and the like may be mixed with the above pentanes as a main component so as to be used.
  • pentanes easily inhibit the resin particles from foaming when the resin particles are discharged to water flow from small holes of the die, the pentanes are suitably used.
  • the amount of the foaming agent contained in the polystyrene resin is in a range of from 3 parts by mass to 10 parts by mass, and more preferably in a range of from 4 parts by mass to 7 parts by mass, based on 100 parts by mass of the polystyrene resin.
  • foamable polystyrene resin particles of the present invention in addition to the flame retardant and the foaming agent, additives that are generally used for producing foamable polystyrene resin particles, for example, a foam-nucleating agent such as talc, calcium silicate, synthesized or naturally generated silicon dioxide, ethylene bis stearamide, or a methacrylic acid ester-based copolymer; a flame-retarding aid such as a diphenyl alkane or a diphenyl alkene; a colorant such as carbon black, iron oxide, or graphite; an antioxidant such as a phenol-based antioxidant, sulfur-based antioxidant, or a phosphorous-based antioxidant; a stabilizer such as hindered amines; and an ultraviolet absorber, can be optionally added to the polystyrene resin.
  • a foam-nucleating agent such as talc, calcium silicate, synthesized or naturally generated silicon dioxide, ethylene bis stearamide, or a meth
  • the foamable polystyrene resin particles of the present invention are produced using the production apparatus shown in FIG. 1 , first, the polystyrene resin as a raw material, the flame retardant, the foam-nucleating agent, and desired additives that are optionally added are weighed, and introduced into the extruder 1 from the raw material supply hopper 3 .
  • the polystyrene resin as a raw material may be introduced from a single raw material supply hopper after being sufficiently mixed in advance by being made into a pellet or granules.
  • the polystyrene resin may be introduced from a plurality of raw material supply hoppers in which the supplication amount has been adjusted for each lot, and the supplied resins may be mixed in the extruder.
  • the recycled raw materials of a plurality of lots it is preferable to sufficiently mix the raw materials of the plurality of lots in advance and remove foreign substances beforehand by using an appropriate sorting means such as magnetic sorting, sieving, gravity sorting, or blowing sorting.
  • a master batch material containing a predetermined level of the flame retardant in a resin when the flame retardant described above is added, it is preferable to use a master batch material containing a predetermined level of the flame retardant in a resin, supply this master batch material into the resin supply device together with the polystyrene resin, and melt and knead the material and the resin in the device.
  • supplying the master batch material containing a predetermined level of the flame retardant in a resin into the resin supply device together with the polystyrene resin, and melting and kneading the material and the resin in the device it is possible to cause the flame retardant to be contained more evenly in the resin particles.
  • the polystyrene resin, the flame retardant, the foaming aid, and other additives are supplied into the extruder 1 , and then resin is melted by heating. Thereafter, while the flame retardant-containing molten resin is transported to the die 2 , a foaming agent is pushed into the molten resin from the foaming agent supply port 5 by the high-pressure pump 4 , whereby the flame retardant-containing molten resin is mixed with the foaming agent.
  • the melt While being further kneaded, the melt is then moved to the leading end side through a screen for removing foreign substances that is optionally provided in the extruder 1 , whereby the melt to which the foaming agent has been added is extruded from small holes of the die 2 provided to the leading end of the extruder 1 .
  • the resin discharge surface in which the small holes of the die 2 are bored is disposed in the cutting chamber 7 into which the cooling water is circulatively supplied.
  • the cutter 6 is rotatably provided so as to be able to cut the resin extruded from the small holes of the die 2 .
  • the formed foamable polystyrene resin particles are transported to the dehydrating drier 10 with a solid-liquid separation function from the cutting chamber 7 along with the flow of the cooling water.
  • the foamable polystyrene resin particles are separated from the cooling water, and dehydrated and cooled.
  • the dried foamable polystyrene resin particles are stored in the storage container 11 .
  • the foamable polystyrene resin particles produced by the process for producing foamable polystyrene resin particles described above are obtained by granulating the polystyrene resin containing the flame retardant and the foaming agent.
  • the flame retardant used for the foamable polystyrene resin particles of the present invention is highly safe for the environment and living organisms.
  • a tetrabromobisphenol A derivative can impart a sufficient flame-retarding performance, and this derivative is highly safe for the environment and living organisms. Therefore, the tetrabromobisphenol A derivative can be used for producing flame-retarding polystyrene resin foam-molded articles for various uses.
  • the details of the flame-retarding foamable polystyrene resin particles, the foamable polystyrene resin particles for producing a heat-insulating material for building materials, the foamable polystyrene resin particles for producing a banking member, and the foamable polystyrene resin particles for producing a vehicle interior material of the present invention, which are produced by the method described above, will be described respectively.
  • the flame retardant has a bromine atom in a molecule, contains less than 70% by mass of bromine, and has a benzene ring in a molecule, and has a 5% by mass decomposition temperature in a range of from 200° C. to 300° C.
  • a ratio (B/A) between (A) the amount of the flame retardant contained in the total foamable polystyrene resin particles and (B) the amount of the flame retardant contained in the surface of the resin particles is in a range of from 0.8 to 1.2.
  • the flame retardant is evenly contained in the resin particles.
  • the ratio (B/A) is more preferably in a range of from 0.9 to 1.1, and even more preferably in a range of from 0.95 to 1.05. If the ratio (B/A) is out of the range of from 0.8 to 1.2, there is a possibility that the mechanical strength, moldability, exterior, and flame retardancy of the obtained flame-retarding polystyrene resin foam-molded article will deteriorate.
  • the ratio (B/A) between (A) the amount of the flame retardant contained in the total resin particles and (B) the amount of the flame retardant contained in the surface of the resin particles is in a range of from 0.8 to 1.2. Consequently, the flame retardant is evenly distributed in the resin particles. Therefore, compared to a case where the flame retardant is unevenly distributed in the resin particles, the mechanical strength of the obtained flame-retarding polystyrene resin foam-molded article is further increased, and the moldability and exterior of the obtained foam-molded article are superior.
  • the flame retardant-containing foamable polystyrene resin particles that are obtained by the above-described production method according to the present invention are prefoamed by heating by means of vapor heating, by using devices and techniques that are known in the field of producing resin foam-molded articles, whereby flame-retarding polystyrene resinprefoamed particles are obtained. These prefoamed particles are prefoamed so as to have bulk density equivalent to the density of a foam-molded article to be produced.
  • the bulk density is not limited, but generally, the bulk density is in a range of from 0.010 g/cm 3 to 0.033 g/cm 3 , and preferably in a range of from 0.015 g/cm 3 to 0.025 g/cm 3 .
  • the bulk density of the polystyrene resinprefoamed particles refers to density measured in the following manner.
  • Wg of the polystyrene resin prefoamed particles are collected as a measurement sample, and the measurement sample is caused to fall into a graduated cylinder by gravity. Thereafter, the bottom of the graduated cylinder is tapped so as to even out an apparent volume (V) cm 3 of the sample, and the mass and volume thereof are measured, whereby the bulk density of the polystyrene resin prefoamed particles is measured based on the following formula.
  • the bulk foaming factor of the prefoamed particles is a numerical value calculated by the following formula.
  • the polystyrene resinprefoamed particles are filled in a cavity of a mold, followed by in-mold foam molding by heating by means of vapor heating or the like, whereby a flame-retarding polystyrene resin foam-molded article is produced.
  • the density of the flame-retarding polystyrene resin foam-molded article of the present invention is not particularly limited, but the density is generally in a range of from 0.010 g/cm 3 to 0.033 g/cm 3 , and preferably in a range of from 0.015 g/cm 3 to 0.025 g/cm 3 .
  • the density of the polystyrene resin foam-molded article is density measured by the method disclosed in JIS K7122: 1999 “Measurement of apparent density of foamed plastic and rubber”.
  • a test piece of 50 cm 3 or larger (100 cm 3 or larger in case of a semi-hard or soft material) is cut such that the original cell structure of the material is not changed.
  • the mass thereof is measured, and the density of the foam-molded article is calculated by the following formula.
  • Density(g/cm 3 ) mass of test piece(g)/volume of test piece(cm 3 )
  • a test piece for adjusting test specimen conditions and for measurement is a test piece that is cut from a sample which has been 72 hours or longer since it was molded, and left as is for 16 hours or longer in atmospheric conditions of 23° C. ⁇ 2° C. ⁇ 50% ⁇ 5% or 27° C. ⁇ 2° C. ⁇ 65% ⁇ 5%.
  • the foaming factor of the foam-molded article is a numerical value calculated from the following formula.
  • Foaming factor(fold) 11/density(g/cm 3 )
  • the flame retardant has a bromine atom in a molecule, contains less than 70% by mass of bromine, has a benzene ring in a molecule, and has a 5% by mass decomposition temperature in a range of from 200° C. to 300° C.
  • the flame retardant is evenly contained in the resin particles. If the flame retardant is unevenly contained in the resin particles, there is a possibility that the mechanical strength, moldability, dimensional stability, exterior, and flame retardancy of the obtained polystyrene resin foam-molded article will deteriorate.
  • the flame retardant is evenly distributed in the resin particles. Consequently, compared to a case where the flame retardant is unevenly distributed in the resin particles, the mechanical strength of the obtained foam-molded article (insulating material for building materials) is further increased, and the moldability and dimensional stability of the obtained insulating material for building materials, banking member, and vehicle interior material are also superior.
  • the total amount of the aromatic organic compounds contained in the obtained foamable polystyrene resin particles for producing a heat-insulating material for building materials, foamable polystyrene resin particles for producing a banking member, and foamable polystyrene resin particles for producing a vehicle interior material can be set to less than 500 ppm.
  • the total amount of the contained aromatic organic compounds is set to preferably 450 ppm or less, and more preferably 400 ppm or less. If the total amount of the contained aromatic organic compounds is small, the mechanical strength of the obtained insulating material for building materials, the banking member, and the vehicle interior material is increased, and the rate of dimensional change is reduced.
  • the total amount of the contained aromatic organic compounds is a value measured by the following ⁇ Method of Measuring Amount of Contained Volatile Organic Compounds (VOC)>.
  • the foamable polystyrene resin particles (1 g) are weighed, and 1 ml of a dimethylformamide solution containing 0.1% by volume of cyclopentanol is further added thereto as an internal standard solution. Thereafter, dimethylformamide is added to the dimethylformamide solution so as to prepare 25 ml of measurement solution, and 1.8 ⁇ l of this measurement solution is supplied to a sample vaporizing chamber at 230° C., thereby obtaining charts of respective volatile organic compounds detected by gas chromatography.
  • the amount of the volatile organic compounds is calculated respectively from the respective charts, thereby calculating the amount of the volatile organic compounds in the foamable polystyrene resin particles.
  • the total amount of the respective volatile organic compounds corresponding to the above-described aromatic organic compounds is taken as the “total amount of contained aromatic organic compounds”.
  • the foamable polystyrene resin particles for producing a heat-insulating material for building materials, the foamable polystyrene resin particles for producing a banking member, and the foamable polystyrene resin particles for producing vehicle interior material which are obtained by the production method according to the present invention, are prefoamed by being heated with vapor heating, by using devices and techniques known in the field of producing resin foam-molded articles, thereby producing flame-retarding polystyrene-based prefoamed particles (hereinafter, written as prefoamed particles). These prefoamed particles are prefoamed so as to have bulk density equivalent to the density of a foam-molded article (insulating material for building materials) to be produced.
  • the bulk density is not limited. However, in a case of prefoamed particles for producing a heat-insulating material for building materials and for producing a banking member, the bulk density is generally in a range of from 0.010 g/cm 3 to 0.050 g/cm 3 , and preferably in a range of form 0.015 g/cm 3 to 0.033 g/cm 3 .
  • the bulk density is generally in a range of from 0.015 g/cm 3 to 0.066 g/cm 3 , and preferably in a range of from 0.015 g/cm 3 to 0.050 g/cm 3 .
  • the prefoamed particles are filled in a cavity of a mold and undergo in-mold foam molding by being heated with vapor heating or the like, by using devices and techniques known in the field of producing resin foam-molded articles, whereby a heat-insulating material for building materials, a banking member, and a vehicle interior material formed of flame-retarding polystyrene resin foam-molded articles are produced.
  • the density of the insulating material for building materials and the banking member of the present invention is generally in a range of from 0.010 g/cm 3 to 0.050 g/cm 3 , and preferably in a range of form 0.015 g/cm 3 to 0.033 g/cm 3 .
  • the density of the vehicle interior material of the present invention is generally in a range of from 0.015 g/cm 3 to 0.066 g/cm 3 , and preferably in a range of from 0.015 g/cm 3 to 0.055 g/cm 3 .
  • the average chord length of bubbles of a foam-molded article that is foamed 40-fold in terms of the foaming factor is preferably in a range of from 50 ⁇ m to 350 ⁇ m, and more preferably in a range of from 60 ⁇ m to 300 ⁇ m.
  • the average chord length of bubbles is average chord length of bubbles of a foam-molded article that is measured by the following method.
  • the average chord length of bubbles of a foam-molded article refers to a length measured based on an ASTM D2842-69 test method. Specifically, a foam-molded article is cut into approximately two equal parts, and the cut plane is photographed by being magnified 100 times by using a scanning electron microscope (product name “S-3000N” manufactured by Hitachi, Ltd.). The photographed image is printed on a sheet of A4 paper, and a straight line having a length of 60 mm is drawn at an arbitrary site. From the number of bubbles on this straight line, an average chord length (t) of bubbles is calculated by the following formula.
  • the bubbles are also included in the number of bubbles.
  • both ends of the straight line are positioned inside the bubbles without passing through the bubbles, the bubbles in which both ends of the straight line are positioned are also included in the number of bubbles.
  • the average chord length is also calculated at five arbitrary sites in the photographed image in the same manner as described above, and an arithmetic mean value of these average chord lengths is taken as the average chord length of bubbles of the foam-molded article.
  • the shape, dimension, and the like of the banking member are not particularly limited and appropriately determined according to the construction method or scale of the bank to be carried out. That is, the banking member can be formed into various sizes or shapes, such as a thick plate shape, a block shape, and a shape having engagement grooves or projections.
  • the average chord length of bubbles of a foam-molded article that is foamed 50-fold in terms of the foaming factor is preferably in a range of from 40 ⁇ m to 200 ⁇ m, and more preferably in a range of from 50 ⁇ m to 150 ⁇ m.
  • an oxygen index is 26 or greater. If the oxygen index is less than 26, there is a possibility that sufficient flame retardancy will not be obtained.
  • the average chord length of a foam-molded article that is foamed 40-fold in terms of the foaming factor is preferably in a range of from 40 ⁇ m to 350 ⁇ m, and more preferably in a range of from 50 ⁇ m to 300 ⁇ m.
  • the entire surface of the foamable polystyrene resin particles was evenly covered with 0.03 parts by mass of polyethylene glycol, 0.15 parts by mass of zinc stearate, 0.05 parts by mass of stearic acid monoglyceride, and 0.05 parts by mass of hydroxy stearic acid triglyceride based on 100 parts by mass of the obtained foamable polystyrene resin particles.
  • the foamable polystyrene resin particles produced as described above were placed in a cool box at 15° C. and left as they were for 72 hours. Thereafter, the particles were supplied to a cylindrical batch-type pre-foaming machine, followed by heating by means of vapor at a blowing pressure of 0.05 MPa, thereby obtaining prefoamed particles.
  • the bulk density of the obtained prefoamed particles was 0.015 g/cm 3 (67-fold in terms of the bulk foaming factor).
  • the obtained prefoamed particles were left as they were for 24 hours in a room temperature atmosphere and then filled in a mold having a rectangular cavity of a length of 400 mm ⁇ a width of 300 mm ⁇ a height of 50 mm.
  • the inside of the cavity of the mold was heated for 20 seconds at a gauge pressure of 0.08 MPa, followed by cooling until the internal pressure of the cavity of the mold became 0.01 MPa, and the mold was opened to take out a rectangular foam-molded article of a length of 400 mm ⁇ a width of 300 mm ⁇ a height of 50 mm.
  • the density of the obtained foam-molded article was 0.015 g/cm 3 (67-fold in terms of the foaming factor).
  • the polystyrene resin, the foamable polystyrene resin particles, the prefoamed particles, and the foam-molded article of Example 1 produced in the above method were subjected to the following tests for evaluation.
  • a method of checking the amount of the flame retardant contained in the total foamable polystyrene resin particles and in the surface thereof for example, a method of quantitatively analyzing the amount of bromine contained in a flame retardant molecule by means of fluorescent X-ray analysis and calculating the amount of the contained flame retardant from the value obtained by the analysis by the following formula is exemplified.
  • Amount of contained flame retardant(% by mass) measured value of the amount of contained bromine ⁇ (molecular weight of total flame retardant ⁇ element content of bromine in total flame retardant)
  • a method of measuring a ratio (B/A) between (A) the amount of the flame retardant contained in the total foamable polystyrene resin particles and (B) the amount of the flame retardant contained in the surface of the resin particles will be described below.
  • the obtained polystyrene resin foam-molded article was dried at 50° C. for 24 hours, and then 2 g of a sample resin obtained from a polystyrene resin foam-molded article 21 was subjected to hot pressing at 190° C. as shown in FIG. 2 , thereby preparing a tablet of 35 mm ⁇ . After the mass of this tablet was measured, basis weight was calculated, and the amount of bromine contained in the resin was calculated by setting a balancing component to PS and performing an order analysis to measure the bromine amount by means of fluorescent X-ray analysis. From the obtained amount of bromine contained, the amount of bromine contained was calculated by the following formula, and the result was taken as (A) the amount of a flame retardant contained in the total resin particles.
  • Amount of contained flame retardant(% by mass) measured value of amount of contained bromine ⁇ (molecular weight of total flame retardant/element content of bromine in total flame retardant)
  • an outermost surface portion 22 of the foam-molded article was cut to a thickness of 0.3 mm with a ham slicer (manufactured by FIJISHIMA KOKI CO., LTD: FK-18N model), and 2 g of a sample resin obtained from the outermost surface portion 22 of the foam-molded article was subjected to hot pressing at 190° C., thereby preparing a tablet of 35 mm ⁇ .
  • basis weight was calculated, and amount of bromine contained in the resin was calculated by setting a balancing component to PS and performing an order analysis to measure the bromine amount by means of fluorescent X-ray analysis. From the obtained amount of bromine contained, the amount of the contained flame retardant was calculated by the following formula, and the result was taken as (B) the amount of a flame retardant contained in the surface of the resin particles.
  • Amount of contained flame retardant(% by mass) measured value of amount of contained bromine ⁇ (molecular weight of total flame retardant/element content of bromine in total flame retardant)
  • Measurement device fluorescent X-ray analyzer manufactured by Rigaku Corporation RIX-2100
  • X-ray tube vertical Rh/Cr tube (3/2.4 kW) analysis diameter: 30 mm ⁇ slit: standard diffraction crystal:
  • LiF detector SC measurement mode: qualitative analysis (FP thin film method-BrPS30-balancing component C8H8)
  • the density of the polystyrene resin foam-molded article 21 as a measurement sample was set to 0.02 g/cm 3 (50-fold in terms of the foaming factor).
  • the density of the molded article 21 was less than 0.02 g/cm 3 due to defective foamability, the molded article 21 having minimum density was used as a measurement sample.
  • the foamable polystyrene resin particles obtained in examples (and comparative examples) were stored for 72 hours in a cool box at 15° C., and then supplied to a cylindrical batch type pre-foaming machine.
  • the particles were heated for 2 minutes by vapor at an injection vapor pressure of 0.05 MPa, the bulk foaming factor of the obtained prefoamed particles were measured in the following manner, and beads foamability was evaluated based on the following criteria.
  • the polystyrene resinprefoamed particles were filled in a mold of a foam molding machine, and the particles were subjected to secondary foaming using vapor, thereby obtaining a cuboidal foam-molded article of a length of 400 mm ⁇ a width of 300 mm ⁇ a thickness of 50 mm.
  • the exterior of the foam-molded article was visually observed to evaluate the exterior of the foam-molded article based on the following criteria.
  • test pieces five test pieces having a thickness of 10 mm, a length of 200 mm, and a width of 25 mm were cut from a foam-molded article sample, and a prescribed ignition limit pointing line and a combustion limit pointing line were drawn in the test pieces. After the test pieces were combusted to the ignition limit pointing line by using a candle for a fire source, the flame was set back, and the time (sec) from the moment of the setting back and to the extinguishment of the flame was measured to evaluate flame retardancy based on the following criteria.
  • Criterion A was not satisfied, or a self-extinguishing property was not observed.
  • a test piece with a size of a thickness of 10 mm ⁇ a length of 150 mm ⁇ a width of 10 mm was cut from the obtained foam-molded article by using a vertical cutter and cured in an oven at 50° C. for 7 days, and then the condition of the test piece was adjusted for 4 days at 23° C. and a relative humidity of 50%.
  • the oxygen index was measured based on JIS K7201, and the flame retardancy was evaluated based on the following criteria.
  • a cuboidal test piece having a length of 200 mm ⁇ a width of 200 mm ⁇ a thickness of 25 mm was cut from a foam-molded article. Thereafter, the thermal conductivity of this test piece was measured at a measurement temperature of 23° C. by a method using a planar heat flow meter based on JIS A1412, and the insulating property of the foam-molded article was judged based on the following criteria.
  • a flame retardant (20 mg) was collected as a sample, and the mass reduction ratio of the sample was measured using a TG/DTA 300 model (manufactured by SEIKO Electronics industrial Co., Ltd.) which is a differential heat and calorie simultaneous measurement device, under a condition of a nitrogen gas amount of 30 ml/min, a heating temperature of 10° C./min, and a measurement temperature of 30° C. to 800° C. From this measurement, a graph of which a vertical axis indicated the mass reduction rate and a horizontal axis indicated the temperature was obtained. Based on this graph, a temperature at the time when the mass reduction ratio of the sample had reached 5% was taken as the 5% by mass decomposition temperature.
  • Foamable polystyrene resin particles (1 g) were accurately weighed, and 1 ml of a dimethylformamide solution containing 0.1% by volume of cyclopentanol was added thereto as an internal standard solution. Thereafter, dimethylformamide was further added to the dimethylformamide solution so as to prepare 25 ml of a measurement solution.
  • This measurement solution (1.8 ⁇ l) was supplied to the sample vaporizing chamber at 230° C., thereby obtaining the respective charts of volatile organic compounds which were detected by gas chromatography (manufactured by Shimadzu Corporation, product name of “GC-14A”) under the following measurement conditions.
  • the amount of the volatile organic compounds were calculated respectively from the respective charts, thereby calculating the amount of the volatile organic compounds in the foamable polystyrene particles.
  • a foam-molded article that was foamed 67-fold in terms of the foaming factor was produced in the same manner as in Example 1, except that tetrabromobisphenol A-bis(2,3-dibromopropyl ether) (manufactured by DAI-ICHI KOGYO SEIYAKU CO., LTD.) was used in the same amount, as a flame retardant.
  • a foam-molded article that was foamed 67-fold in terms of the foaming factor was produced in the same manner as in Example 1, except that tetrabromobisphenol A-bis(allyl ether) (manufactured by DAI-ICHI KOGYO SEIYAKU CO., LTD.) was used in the same amount, as a flame retardant.
  • a foam-molded article that was foamed 67-fold in terms of the foaming factor was produced in the same manner as in Example 1, except that 3.2 parts by mass of tetrabromobisphenol A-bis(2,3-dibromopropyl ether) was mixed with 0.3 parts by mass of tetrabromobisphenol A-bis(allyl ether) so as to be used as a flame retardant.
  • a foam-molded article was produced in the same manner as in Example 1, except that the bulk foaming factor of prefoamed particles was set to 40-fold, and that the foaming factor of the foam-molded article was set to 40-fold.
  • the average chord length of bubbles of the foam-molded article was 183 ⁇ m.
  • a foam-molded article that was foamed 67-fold in terms of the foaming factor was produced in the same manner as in Example 1, except that the amount of the flame retardant A mixed was set to 5.0 parts by mass.
  • a foam-molded article was produced in the same manner as in Example 1, except that hexabromocyclodecane (manufactured by DAI-ICHI KOGYO SEIYAKU CO., LTD.) was used in the same amount, as a flame retardant.
  • a foam-molded article was produced in the same manner as in Example 1, except that tris-(2,3-dibromopropyl)isocyanurate (manufactured by Nippon Kasei Chemical Co., Ltd) was used in the same amount, as a flame retardant.
  • a foam-molded article was produced in the same manner as in Example 1, except that pentabromobenzyl acrylate (manufactured by DAI-ICHI KOGYO SEIYAKU CO., LTD.) was used in the same amount, as a flame retardant.
  • a foam-molded article was produced in the same manner as in Example 1, except that tris(tribromoneopentyl)phosphate (manufactured by DAIHACHI CHEMICAL INDUSTRY CO, LTD) was used in the same amount, as a flame retardant.
  • a foam-molded article that was foamed 67-fold in terms of the foaming factor was produced in the same manner as in Example 1, except that foamable polystyrene resin particles were obtained by a suspension polymerization method as a process for producing foamable polystyrene resin particles.
  • Tricalcium phosphate 120 g (manufactured by Taihei Chemical Industrial Co., Ltd.), 4 g of sodium dodecylbenzenesulfonate, 140 g of benzoyl peroxide (purity of 75%), 30 g of t-butylperoxy-2-ethylhexyl monocarbonate, 40 kg of ion exchange water, and 40 kg of a styrene monomer were introduced to an autoclave equipped with a stirrer having an internal volume of 100 L, followed by dissolution and dispersion under stirring at 100 rpm, thereby forming a suspension.
  • the internal temperature of the autoclave was raised to 90° C. while the stirring blade performed stirring at 100 rpm, and then the temperature was kept at 90° C. for 6 hours.
  • the internal temperature of the autoclave was further raised to 120° C., and the temperature was kept at 120° C. for 2 hours.
  • the internal temperature of the autoclave was cooled to 25° C., the content of the autoclave was taken out, followed by dehydration, drying, and classification, thereby obtaining styrene-based resin particles having a particle size of 0.6 mm to 0.85 mm and a weight average molecular weight of 300,000.
  • an emulsion prepared in advance was added to the reactor kept at 75° C.
  • This emulsion was obtained by adding 88 g of benzoyl peroxide (purity of 75%) as a polymerization initiator and 5 kg of styrene in which 50 g of t-butylperoxy-2-ethylhexyl monocarbonate had been dissolved to a dispersion containing 6 kg of pure water, 2 g of sodium dodecylbenzenesulfonate, and 20 g of magnesium pyrophosphate, and emulsifying this mixture by means of stirring with a homomixer.
  • the reactor was held as it was for 30 minutes such that the styrene and the polymerization initiator were absorbed well into the styrene-based resin particles, and then 28 kg of styrene was continuously added dropwise thereto for 160 minutes while the internal temperature of the autoclave was raised from 75° C. to 108° C. at a rate of 0.2° C./min.
  • Diisobutyl adipate (308 g) (manufactured by Taoka Chemical Co., Ltd., product name: D14A) was added to a dispersion containing 2 kg of hot water and 0.8 g of sodium dodecylbenzenesulfonate, followed by stirring with a homomixer, thereby preparing an emulsion.
  • the autoclave was cooled to 90° C. at a rate of 1° C./min, and the above emulsion prepared in advance was added to the reactor.
  • 30 minutes after the addition of the emulsion 1540 g of tetrabromobisphenol A-bis(2,3-dibromo-2-methylpropyl ether) (manufactured by DAIHACHI CHEMICAL INDUSTRY CO, LTD) was added thereto as a flame retardant, and then the reactor was sealed.
  • a foam-molded article that was foamed 67-fold in terms of the foaming factor was produced in the same manner as in Comparative Example 5, except that tetrabromobisphenol A-bis(allyl ether) (manufactured by DAIHACHI CHEMICAL INDUSTRY CO, LTD) was used in the same amount, as a flame retardant.
  • Examples 1 to 6 of the present invention that used flame retardants A to C having a bromine atom in an example molecule, containing less than 70% by mass of bromine, having a benzene ring in a molecule, and having a 5% by mass decomposition temperature in a range of from 200° C. to 300° C. were excellent in any of the beads foamability, the flame retardancy, and the exterior of a foamed article.
  • Comparative Example 1 that used a flame retardant D containing bromine as much as 75% by mass and not having a benzene ring in a molecule was poor in the beads foamability, and the exterior of the foamed article also slightly deteriorated.
  • Comparative Example 2 that used a flame retardant E not having a benzene ring in a molecule exhibited defective beads foamability, and the exterior of the foamed article was also defective.
  • Comparative Example 3 that used a flame retardant F containing a large amount of bromine at 75% by mass and having a 5% by mass decomposition temperature of higher than 300° C. exhibited slightly defective beads foamability and defective flame retardancy, and the exterior of the foamed article was slightly defective.
  • Comparative Example 4 that used a flame retardant G containing a large amount of bromine at 75% by mass, not having a benzene ring in a molecule, and having a 5% by mass decomposition temperature of higher than 300° C. was defective in all of the beads foamability, the flame retardancy, and the exterior of the foamed article.
  • the present invention relates to a flame-retarding polystyrene resin foam-molded article that uses a flame retardant which is highly safe for the environment and living organisms, has a sufficient flame-retarding performance, and is excellent in mechanical strength, moldability, and exterior, and to foamable polystyrene resin particles used for producing such a molded product and a process for production thereof.
  • the polystyrene resin foam-molded article of the present invention is suitably used for foam-molded articles that are required to have flame retardancy, for example, building materials or vehicle interior materials.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
US13/504,072 2009-10-27 2010-10-27 Foamable polystyrene resin particles and process for production thereof, polystyrene resin prefoamed particles, polystyrene resin foam-molded article, heat-insulating material for building material, banking member, and vehicle interior material Abandoned US20120214885A1 (en)

Applications Claiming Priority (9)

Application Number Priority Date Filing Date Title
JP2009246290A JP5750221B2 (ja) 2009-10-27 2009-10-27 難燃剤含有発泡性ポリスチレン系樹脂粒子とその製造方法、難燃性ポリスチレン系樹脂予備発泡粒子及び難燃性ポリスチレン系樹脂発泡成形体
JP2009-246290 2009-10-27
JP2009-246292 2009-10-27
JP2009-246293 2009-10-27
JP2009246293A JP2011093950A (ja) 2009-10-27 2009-10-27 車両内装材製造用発泡性ポリスチレン系樹脂粒子とその製造方法、車両内装材製造用予備発泡粒子及び車両内装材
JP2009-246291 2009-10-27
JP2009246291A JP2011093948A (ja) 2009-10-27 2009-10-27 建材用断熱材製造用発泡性ポリスチレン系樹脂粒子とその製造方法、建材用断熱材製造用予備発泡粒子及び建材用断熱材
JP2009246292A JP2011093949A (ja) 2009-10-27 2009-10-27 盛土用部材製造用発泡性ポリスチレン系樹脂粒子とその製造方法、盛土用部材製造用予備発泡粒子及び盛土用部材
PCT/JP2010/069053 WO2011052631A1 (ja) 2009-10-27 2010-10-27 発泡性ポリスチレン系樹脂粒子とその製造方法、ポリスチレン系樹脂予備発泡粒子、ポリスチレン系樹脂発泡成形体、建材用断熱材、盛土用部材及び車両内装材

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2010/069053 A-371-Of-International WO2011052631A1 (ja) 2009-10-27 2010-10-27 発泡性ポリスチレン系樹脂粒子とその製造方法、ポリスチレン系樹脂予備発泡粒子、ポリスチレン系樹脂発泡成形体、建材用断熱材、盛土用部材及び車両内装材

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US15/098,702 Continuation-In-Part US20160229974A1 (en) 2009-10-27 2016-04-14 Foamable polystyrene resin particles and polystyrene resin prefoamed particles

Publications (1)

Publication Number Publication Date
US20120214885A1 true US20120214885A1 (en) 2012-08-23

Family

ID=43922056

Family Applications (1)

Application Number Title Priority Date Filing Date
US13/504,072 Abandoned US20120214885A1 (en) 2009-10-27 2010-10-27 Foamable polystyrene resin particles and process for production thereof, polystyrene resin prefoamed particles, polystyrene resin foam-molded article, heat-insulating material for building material, banking member, and vehicle interior material

Country Status (5)

Country Link
US (1) US20120214885A1 (ja)
EP (1) EP2495277B1 (ja)
CN (2) CN102686654A (ja)
TW (1) TWI439503B (ja)
WO (1) WO2011052631A1 (ja)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013023508A (ja) * 2011-07-15 2013-02-04 Kaneka Corp 難燃性発泡性スチレン系樹脂粒子の製造方法
US8772362B1 (en) 2013-02-15 2014-07-08 Nexkemia Petrochimie Inc. Expanded polystyrene made using D-limonene as a plasticizer
WO2017063870A1 (de) * 2015-10-16 2017-04-20 Alois Edler Verfahren und vorrichtung zum herstellen eines als werkstoff für eine wärmedämmschüttung vorgesehenes polystyrol-granulat
US9644079B2 (en) 2013-02-15 2017-05-09 Nexkemia Petrochemicals, Inc. Shaping of expanded polystyrene made using D-limonene as a plasticizer
US20180244884A1 (en) * 2015-10-30 2018-08-30 Kaneka Corporation Styrene resin extruded foam body and method for producing same
US20180251620A1 (en) * 2015-11-05 2018-09-06 Kaneka Corporation Styrene resin extruded foam and method for producing same
EP3481891B1 (en) 2016-07-08 2020-04-08 Versalis S.p.A. Expandable compositions containing aromatic vinyl polymers having self-extinguishing properties and improved processability
KR20200041885A (ko) * 2017-08-17 2020-04-22 다이이치 고교 세이야쿠 가부시키가이샤 난연성 발포 스티렌계 수지 조성물
CN113502080A (zh) * 2021-07-29 2021-10-15 亚士创能科技(乌鲁木齐)有限公司 阻燃涂料、石墨聚苯阻燃颗粒、石墨聚苯阻燃板及制备方法
EP3708936B1 (de) * 2019-03-15 2024-04-17 Polymetrix AG Verfahren zum recycling von polyolefinen

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20160229974A1 (en) * 2009-10-27 2016-08-11 Sekisui Plastics Co., Ltd. Foamable polystyrene resin particles and polystyrene resin prefoamed particles
US10358538B2 (en) 2009-10-27 2019-07-23 Sekisui Plastics Co., Ltd. Foamable polystyrene resin particles and polystyrene resin prefoamed particles
JP5679353B2 (ja) * 2012-10-09 2015-03-04 第一工業製薬株式会社 粒状難燃剤組成物および熱可塑性樹脂組成物
WO2016017813A1 (ja) * 2014-07-31 2016-02-04 積水化成品工業株式会社 スチレン系樹脂発泡性粒子及びその製造方法、発泡粒子、発泡成形体並びにその用途
JP6405781B2 (ja) * 2014-08-08 2018-10-17 株式会社ジェイエスピー 発泡性スチレン系樹脂粒子及びその製造方法
CN105374426A (zh) * 2015-11-24 2016-03-02 安徽南洋新材料科技股份有限公司 一种高韧性耐磨耐撕裂阻燃电缆
JP6135791B2 (ja) * 2016-03-30 2017-05-31 株式会社カネカ 難燃性発泡性スチレン系樹脂粒子の製造方法
CN109880248B (zh) * 2019-02-23 2022-03-25 山东兄弟科技股份有限公司 一种甲基八溴醚阻燃聚苯乙烯复合材料及其制备方法

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007169408A (ja) * 2005-12-21 2007-07-05 Sekisui Plastics Co Ltd スチレン系樹脂発泡性粒子とその製造方法及び型内発泡成形品

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61191237A (ja) 1985-02-18 1986-08-25 古河電池株式会社 蓄電池用充電器
JPS63172744A (ja) 1987-01-13 1988-07-16 Teijin Chem Ltd 難燃性発泡スチレン系樹脂の製造方法
JPH08302056A (ja) * 1995-05-12 1996-11-19 Sekisui Chem Co Ltd 難燃性樹脂発泡体の製造方法
ES2151268T3 (es) 1997-05-14 2000-12-16 Basf Ag Polimeros de estireno expandibles que contienen particulas de grafito.
JP4326034B2 (ja) 1997-09-30 2009-09-02 株式会社ジェイエスピー スチレン系発泡性樹脂粒子
JP4006745B2 (ja) 1997-10-31 2007-11-14 日立化成工業株式会社 自己消火性発泡ポリスチレン樹脂粒子の製造方法及び成形品
JP4035979B2 (ja) 2000-10-20 2008-01-23 株式会社カネカ 発泡性ポリスチレン系樹脂粒子及びその製造方法
JP2003064212A (ja) 2001-08-27 2003-03-05 Kanegafuchi Chem Ind Co Ltd 発泡性ポリスチレン系樹脂粒子およびポリスチレン系樹脂発泡成形体
JP2003335891A (ja) 2002-05-21 2003-11-28 Kanegafuchi Chem Ind Co Ltd 発泡性ポリスチレン系樹脂粒子、ポリスチレン系発泡成形体、およびその製造方法
US20050261455A1 (en) * 2002-08-09 2005-11-24 Kaneka Corporation Formable styrenic resin particle, and pre-formed particle and foamed molding using the same
JP2004075952A (ja) * 2002-08-22 2004-03-11 Teijin Chem Ltd 難燃性発泡性ポリスチレン系樹脂組成物およびそれからの成形品
JP5134753B2 (ja) * 2003-11-07 2013-01-30 株式会社カネカ スチレン系樹脂発泡体およびその製造方法
JP4914000B2 (ja) * 2004-11-12 2012-04-11 株式会社ジェイエスピー ポリスチレン系樹脂押出発泡板
JP4937610B2 (ja) * 2005-04-12 2012-05-23 第一工業製薬株式会社 難燃性発泡ポリスチレン系樹脂およびその成形体
DE102005039976A1 (de) * 2005-08-23 2007-03-08 Basf Ag Partikel aus expandierbarem Polystyrol und daraus erhältliche Formteile mit verbessertem Brandverhalten
JP5042654B2 (ja) * 2006-02-07 2012-10-03 株式会社カネカ 熱可塑性樹脂発泡体
JP4864473B2 (ja) * 2006-02-10 2012-02-01 第一工業製薬株式会社 難燃性スチレン系樹脂組成物
JP5248041B2 (ja) * 2007-05-28 2013-07-31 株式会社カネカ 熱可塑性樹脂発泡体
JP4729067B2 (ja) 2008-03-31 2011-07-20 古河電気工業株式会社 電界効果トランジスタ
JP2009246291A (ja) 2008-03-31 2009-10-22 Furukawa Electric Co Ltd:The 面発光レーザアレイ素子
JP5243831B2 (ja) 2008-03-31 2013-07-24 株式会社コベルコ マテリアル銅管 ヒートパイプ用内面溝付管及びヒートパイプ
JP2009246293A (ja) 2008-03-31 2009-10-22 Toda Kogyo Corp 磁気記録用金属磁性粒子粉末及びその製造法、並びに磁気記録媒体
HUE030035T2 (en) * 2009-04-28 2017-04-28 Dai-Ichi Kogyo Seiyaku Co Ltd Flame retardant foamable styrene resin preparation

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007169408A (ja) * 2005-12-21 2007-07-05 Sekisui Plastics Co Ltd スチレン系樹脂発泡性粒子とその製造方法及び型内発泡成形品

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013023508A (ja) * 2011-07-15 2013-02-04 Kaneka Corp 難燃性発泡性スチレン系樹脂粒子の製造方法
US8772362B1 (en) 2013-02-15 2014-07-08 Nexkemia Petrochimie Inc. Expanded polystyrene made using D-limonene as a plasticizer
US9644079B2 (en) 2013-02-15 2017-05-09 Nexkemia Petrochemicals, Inc. Shaping of expanded polystyrene made using D-limonene as a plasticizer
WO2017063870A1 (de) * 2015-10-16 2017-04-20 Alois Edler Verfahren und vorrichtung zum herstellen eines als werkstoff für eine wärmedämmschüttung vorgesehenes polystyrol-granulat
US20180244884A1 (en) * 2015-10-30 2018-08-30 Kaneka Corporation Styrene resin extruded foam body and method for producing same
US20180251620A1 (en) * 2015-11-05 2018-09-06 Kaneka Corporation Styrene resin extruded foam and method for producing same
EP3481891B1 (en) 2016-07-08 2020-04-08 Versalis S.p.A. Expandable compositions containing aromatic vinyl polymers having self-extinguishing properties and improved processability
US11359066B2 (en) 2016-07-08 2022-06-14 Versalis S.P.A. Expandable compositions containing aromatic vinyl polymers having self-extinguishing properties and improved processability
KR20200041885A (ko) * 2017-08-17 2020-04-22 다이이치 고교 세이야쿠 가부시키가이샤 난연성 발포 스티렌계 수지 조성물
EP3670585A4 (en) * 2017-08-17 2021-03-10 Dai-Ichi Kogyo Seiyaku Co., Ltd. FIRE-RESISTANT EXPANDED STYRENE RESIN COMPOSITION
KR102572428B1 (ko) 2017-08-17 2023-08-30 다이이치 고교 세이야쿠 가부시키가이샤 난연성 발포 스티렌계 수지 조성물
EP3708936B1 (de) * 2019-03-15 2024-04-17 Polymetrix AG Verfahren zum recycling von polyolefinen
CN113502080A (zh) * 2021-07-29 2021-10-15 亚士创能科技(乌鲁木齐)有限公司 阻燃涂料、石墨聚苯阻燃颗粒、石墨聚苯阻燃板及制备方法

Also Published As

Publication number Publication date
TWI439503B (zh) 2014-06-01
TW201124462A (en) 2011-07-16
EP2495277A1 (en) 2012-09-05
WO2011052631A1 (ja) 2011-05-05
CN102686654A (zh) 2012-09-19
EP2495277B1 (en) 2021-03-24
CN105542216A (zh) 2016-05-04
EP2495277A4 (en) 2014-05-21

Similar Documents

Publication Publication Date Title
US20120214885A1 (en) Foamable polystyrene resin particles and process for production thereof, polystyrene resin prefoamed particles, polystyrene resin foam-molded article, heat-insulating material for building material, banking member, and vehicle interior material
JP5750221B2 (ja) 難燃剤含有発泡性ポリスチレン系樹脂粒子とその製造方法、難燃性ポリスチレン系樹脂予備発泡粒子及び難燃性ポリスチレン系樹脂発泡成形体
JP4774293B2 (ja) スチレン系樹脂発泡性粒子とその製造方法及び型内発泡成形品
US20120252914A1 (en) Flame-protected polymer foams
US20080058435A1 (en) Halogen-Fere Flame-Retarded Polymer Foams
JP6473675B2 (ja) スチレン系樹脂発泡性粒子及びその製造方法、発泡粒子、発泡成形体並びにその用途
US20160229974A1 (en) Foamable polystyrene resin particles and polystyrene resin prefoamed particles
JP6612634B2 (ja) スチレン系樹脂発泡性粒子、発泡粒子及び発泡成形体
US10358538B2 (en) Foamable polystyrene resin particles and polystyrene resin prefoamed particles
JP6389591B2 (ja) ポリスチレン系樹脂発泡体の製造方法
JP2011093948A (ja) 建材用断熱材製造用発泡性ポリスチレン系樹脂粒子とその製造方法、建材用断熱材製造用予備発泡粒子及び建材用断熱材
JP6407113B2 (ja) スチレン系樹脂発泡成形体及びその製造方法並びにその用途
JP2011094024A (ja) 不燃剤含有発泡性ポリスチレン系樹脂粒子とその製造方法、不燃性ポリスチレン系樹脂予備発泡粒子及び不燃性ポリスチレン系樹脂発泡成形体
JP2011093953A (ja) 床暖房用断熱材製造用発泡性ポリスチレン系樹脂粒子とその製造方法、床暖房用断熱材製造用予備発泡粒子、床暖房用断熱材及び床暖房装置
JP2011093950A (ja) 車両内装材製造用発泡性ポリスチレン系樹脂粒子とその製造方法、車両内装材製造用予備発泡粒子及び車両内装材
JP2012077149A (ja) 発泡性樹脂粒子、その製造方法、予備発泡粒子及び発泡成形体
JP6692219B2 (ja) 発泡性スチレン系樹脂粒子の製造方法
KR20160072411A (ko) 성형성이 우수하고 단열성능과 난연성능이 우수한 발포성 폴리스티렌 입자 및 이의 제조방법
JP2017132971A (ja) スチレン系樹脂発泡粒子及びスチレン系樹脂発泡成形体
JP5909903B2 (ja) 難燃性発泡性スチレン系樹脂粒子の製造方法
JP2011093952A (ja) 貯湯タンク用断熱材製造用発泡性ポリスチレン系樹脂粒子とその製造方法、貯湯タンク用断熱材製造用予備発泡粒子及び貯湯タンク用断熱材
JP2011093949A (ja) 盛土用部材製造用発泡性ポリスチレン系樹脂粒子とその製造方法、盛土用部材製造用予備発泡粒子及び盛土用部材
JP2004217875A (ja) 自己消火型スチレン系樹脂発泡粒子及び自己消火型発泡成形体
JP2011093951A (ja) 屋根下断熱材製造用発泡性ポリスチレン系樹脂粒子とその製造方法、屋根下断熱材製造用予備発泡粒子及び屋根下断熱材
JP6436575B2 (ja) 発泡体及びその製造方法

Legal Events

Date Code Title Description
AS Assignment

Owner name: SEKISUI PLASTICS CO., LTD., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:TARUMOTO, HIROYUKI;CHINOMI, RYOSUKE;REEL/FRAME:028180/0951

Effective date: 20120507

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION